Variant report

Variant	rs17153310
Chromosome Location	chr5:125122497-125122498
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1833703	1.00[AMR][1000 genomes]
rs57673408	1.00[AMR][1000 genomes]
rs58525016	1.00[AMR][1000 genomes]
rs6892385	1.00[AMR][1000 genomes]
rs6892404	1.00[AMR][1000 genomes]
rs73314079	1.00[AMR][1000 genomes]
rs73314081	1.00[AMR][1000 genomes]
rs73314102	1.00[AMR][1000 genomes]
rs73318158	1.00[AMR][1000 genomes]
rs73318193	1.00[AMR][1000 genomes]
rs73320281	1.00[AMR][1000 genomes]
rs73320283	1.00[AMR][1000 genomes]
rs73322941	1.00[AMR][1000 genomes]
rs73322977	1.00[AMR][1000 genomes]
rs7727911	1.00[AMR][1000 genomes]
rs7728069	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030992	chr5:124708549-125391503	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv537892	chr5:124708549-125391503	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv534468	chr5:124943170-125634960	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	esv2758014	chr5:125050863-125287909	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv2759376	chr5:125050863-125287909	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv882829	chr5:125092500-125124027	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv521316	chr5:125111363-125134363	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:125121800-125123200	Enhancers	iPS-20b Cell Line	embryonic stem cell
2	chr5:125121800-125123400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr5:125122000-125122600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr5:125122000-125123400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr5:125122200-125122800	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr5:125122200-125123200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr5:125122400-125123600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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